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Overview
lovance Biotherapeutics is a growing, late-stage company focused on the development and commercialization of novel cancer immunotherapies. lovance is seeking an Investigator I, for the Quality Control Compliance team who will in advance and close QC related investigations. Strong technical writing skills are required. Experience in a CAR-T or TIL environment is a plus.
The ideal candidate will have experience working in a GMP-regulated laboratory with experience in writing investigations.
Shift: Sun. - Wed. 9am - 8pm
Essential Functions and Responsibilities
Required Education, Skills, and Knowledge
Preferred Education, Skills, and Knowledge
The physical demands described here represent those that an employee must meet to perform the essential functions of this job successfully. Reasonable accommodations may be made upon request to enable individuals to perform essential functions. Please contact Human Resources to request an accommodation.
Physical Demands and Activities Required:
Mental:
Work Environment:
The statements contained in this document are intended to describe the general nature and level of work being performed by a colleague assigned to this description. They are not intended to constitute a comprehensive list of functions, duties, or local variances. Management retains the discretion to add or to change the duties of the position at any time.
lovance is committed to cultivating and offering a diverse and inclusive work environment. As an equal opportunity employer, our employees and applicants will be considered without regard to an individual's race, color, religion, sex, pregnancy, national origin, age, physical and mental disability, marital status, sexual orientation, gender identity, gender expression, genetic information, military and veteran status, and any other characteristic protected by applicable law. If you need assistance or accommodation to apply to one of our opportunities, please contact [email protected].
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